Condition

Xia-Gibbs syndrome

Diseases of the Nervous System

Xia-Gibbs syndrome is a rare neurodevelopmental disorder marked by low muscle tone, delayed development and intellectual disability that ranges from mild to severe. Speech is hit hardest: many children say no first word until age two or later, and some never talk. Other features vary from person to person and can include seizures, poor balance and coordination, feeding difficulties, sleep problems including obstructive sleep apnea, short stature, scoliosis and a thin corpus callosum on brain imaging. Some people have distinctive facial features, and some have autism spectrum disorder or attention-deficit/hyperactivity disorder. The syndrome is caused by new variants in the AHDC1 gene, usually producing shortened proteins, and follows an autosomal dominant pattern. Its true frequency is unknown, and it is probably underdiagnosed.

Facts
Classification
Body System
Nervous System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Prevalence Band
Rare (Under 1 in 2000) 3
Sources
1. Xia-Gibbs syndrome (MedlinePlus Genetics)
  • Description
    Xia-Gibbs syndrome is a neurological disorder characterized by weak muscle tone (hypotonia), mild to severe intellectual disability and delayed development.
  • Causes
    Xia-Gibbs syndrome is caused by variants (also known as mutations) in a gene called AHDC1.
  • Inheritance
    Xia-Gibbs syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
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2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:412069 Xia-Gibbs syndrome
Orphadata (Orphanet)ICD-10 cross-reference
Quote, ICD-10 cross-reference
"Reference": "Q87.8", "Source": "ICD-10"
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3. Orphadata (Orphanet): Orphadata epidemiology for ORPHA:412069 AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome
Orphadata (Orphanet)Prevalence, Worldwide
Quote, Prevalence, Worldwide
"PrevalenceClass": "\u003c1 / 1 000 000", "PrevalenceGeographic": "Worldwide"
View the Source
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